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9. Neuroepithelial defects of the inner ear in a new allele of the mouse mutation Ames waltzer. Alagramam KN; Zahorsky-Reeves J; Wright CG; Pawlowski KS; Erway LC; Stubbs L; Woychik RP Hear Res; 2000 Oct; 148(1-2):181-91. PubMed ID: 10978835 [TBL] [Abstract][Full Text] [Related]
10. The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene. Alagramam KN; Murcia CL; Kwon HY; Pawlowski KS; Wright CG; Woychik RP Nat Genet; 2001 Jan; 27(1):99-102. PubMed ID: 11138007 [TBL] [Abstract][Full Text] [Related]
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12. Lim2(To3) transgenic mice establish a causative relationship between the mutation identified in the lim2 gene and cataractogenesis in the To3 mouse mutant. Steele EC; Wang JH; Lo WK; Saperstein DA; Li X; Church RL Mol Vis; 2000 Jun; 6():85-94. PubMed ID: 10851259 [TBL] [Abstract][Full Text] [Related]
13. Ontogeny of hyperactivity and circling behavior in a transgenic insertional mutant mouse. Fitzgerald LW; Ratty AK; Miller KJ; Ellsworth MK; Glick SD; Gross KW Behav Neurosci; 1991 Oct; 105(5):755-63. PubMed ID: 1815622 [TBL] [Abstract][Full Text] [Related]
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15. Human BAC-mediated rescue of the Friedreich ataxia knockout mutation in transgenic mice. Sarsero JP; Li L; Holloway TP; Voullaire L; Gazeas S; Fowler KJ; Kirby DM; Thorburn DR; Galle A; Cheema S; Koenig M; Williamson R; Ioannou PA Mamm Genome; 2004 May; 15(5):370-82. PubMed ID: 15170226 [TBL] [Abstract][Full Text] [Related]
16. Phenotypic and expression analysis of a novel spontaneous myosin VI null mutant mouse. Mochizuki E; Okumura K; Ishikawa M; Yoshimoto S; Yamaguchi J; Seki Y; Wada K; Yokohama M; Ushiki T; Tokano H; Ishii R; Shitara H; Taya C; Kitamura K; Yonekawa H; Kikkawa Y Exp Anim; 2010; 59(1):57-71. PubMed ID: 20224170 [TBL] [Abstract][Full Text] [Related]
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